H18.1
Conditions
Interventions
Group 1: Patients with corneal endothelial dysfunction who have already undergone a 'Maxi-DMEK' or 'Maxi-Rebubbling' procedure
Sponsors
Augenklinik Uniklinik Düsseldorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with corneal endothelial dysfunction previously treated with 'Maxi-DMEK' or 'Maxi-Rebubbling
Exclusion criteria
Exclusion criteria: the abscence of medical documentation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study is designed as a retrospective analysis of pre-existing data obtained from digital patient files. The primary outcome measure is successful graft adhesion without the need for secondary rebubbling (Rebubbling required: Yes/No? If yes, count), and the anterior chamber gas fill percentage on postoperative day 1 | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoints are also evaluated retrospectively based on available measurement data: visual function defined as Best Corrected Visual Acuity (BCVA) in Snellen and logMAR, Central Corneal Thickness (CCT) in µm and the Intraocular Pressure (IOP) in mmHg. These endpoints are assessed preoperatively and 3 months postoperatively. | — |
Countries
Germany
Contacts
Public ContactNieki Marjani
Augenklinik Uniklinik Düsseldorf
Outcome results
None listed